Substituted 1-(4-aminophenly)triazoles and their use as anti-inflammatory agents

ABSTRACT

Compounds of formula I                    
     wherein: 
     R 1  is pyridyl optionally substituted with halogen, C 1-4  alkyl, C 1-4  alkenyl, CN, Me 2 N, CO 2 Me, OMe, aryl, heterocyclyl, or R 4 ; 
     R 2  is CF 3 ; halogen; CN; branched or unbranched C 1-8  alkyl; branched or unbranched C 1-8  alkenyl; C 3-8  cycloalkyl optionally substituted with OH, CN, or methoxy; C 1-8  alkoxy; C 1-4  alkyloxyalkyl; C 1-8  alkylthio; C 1-4  alkylthioalkyl; C 1-8  dialkylamino; C 1-4  dialkylaminoalkyl; CO 2 R 4 ; or aryl connected to the triazole in any position that makes a stable bond and wherein the aryl thereof is optionally substituted with halogen, C 1-4  alkyl, C 1-4  alkenyl, CN, Me 2 N, CO 2 Me, OMe, aryl, heterocyclyl, or R 4 ; 
     L is —NHC(O)—; —NHC(O)O—; —NHC(O)C(O)—; —NHC(S)—; —NH—; —NHC(O)NH—; —NHC(S)NH—; —NHCH 2 —; —NHCH(R 5 )—, wherein R 5  is H, CN, C 1-6  alkyl, C 1-6  alkyloxyalkyl, C 1-6  alkylthioalkyl, C 1-6  alkylsulfinylalkyl, C 1-6  alkylsulfonylalkyl, C 3-6  cycloalkyl, heterocyclyl, or aryl optionally substituted with a halogen, C 1-4  alkyl, CN, Me 2 N, CO 2 Me, or OMe; 
     R 3  is C 1-8  alkyl; C 1-8  alkyloxy; C 1-8  alkylthio; C 1-8  alkylamino; C 1-4  alkoxyalkyl; C 1-4  alkylthioalkyl; C 1-4  alkylaminoalkyl; C 1-4  dialkylalkylaminoalkyl; —CO 2 R 6 ; —N(R 6 ) 2 ; —NH(R 6 ); —C(O)R 6 ; —OR 6 ; S(O) n R 6  wherein n is 0, 1, or 2; —SO 2 NHR 6 ; —SO 2 N(R 6 ) 2 ; or carbocyclyl or heterocyclyl, wherein the carbocyclyl or heterocyclyl thereof is optionally substituted with one or more of the following: halogen, —CN, —NO 2 , —SO 2 NH 2 , or R 6 , wherein R 6  is phenyl, heterocyclyl, C 3-6  cycloalkyl, C 1-6  alkyl, C 2-6  alkenyl, C 1-6  alkyloxyalkyl, C 1-6  alkylthioalkyl, C 1-6  alkyl-sulfinylalkyl, C 1-6  alkylsulfonylalkyl, or C 2-6  alkynyl, and R 6  is optionally substituted with halogen, —OH, alkyloxy, —CN, —COO-lower alkyl, —CONH-lower alkyl, —CON(lower alkyl) 2 , dialkylamino, phenyl, or heterocyclyl; and R 4  is C 1-4  alkyl or C 1-4  alkenyl optionally substituted with carbocyclyl or heterocyclyl, or a pharmaceutically acceptable derivative thereof, pharmaceutical compositions comprising compounds of formula I, and methods of treating an inflammatory disease using compounds of formula I.

BACKGROUND OF THE INVENTION

It has been well established that T-cells play an important role in regulating immune response (F. Powrie and R. L. Coffman, Immunol. Today, 1993, 14, 270). Indeed, activation of T-cells is often the initiating event in many inflammatory and autoimmune diseases. IL-2 is an autocrine growth factor which plays an essential role in the regulation of T-cell activation and proliferation. Clinical studies have shown that interference with IL-2 activity effectively suppresses immune response in vivo (T. A. Waldmann, Immunol. Today, 1993, 14, 264). Accordingly, agents which inhibit IL-2 production are therapeutically useful for selectively suppressing immune response in a patient in need of such immunosuppression.

Previously, others have attempted to interfere with the activity of IL-2 by using cytokine antagonists, monoclonal antibodies, toxins and other biologics which seek to prevent IL-2 from binding to its receptor (G. Mazur and I. Frydecka, Acta Haematol. Pol., 1993, 24, 307, 1993). More recently, others have attempted to inhibit IL-2 production at the T-cell level, for example by blocking the expression of IL-2 mRNA with glucocorticoids or cyclosporin A. However, to date, the reported compounds suffer from several disadvantages such as low potency, poor in vivo activity, toxicity and poor oral bioavailability. Accordingly, a need exists for compounds that can effectively inhibit IL-2 production for preventing and treating immune disorders.

U.S. application Ser. No. 09/324,933 discloses substituted 1-(4-aminophenyl)pyrazoles as anti-inflammatory agents. WO9919303 describes substituted phenyl-, heteroaryl- and heterocyclyl-substituted pyrazoles as useful in the treatment of allergy, inflammatory and autoimmune diseases. WO9951580 describes substituted pyrazoles as inhibitors of cytokine production.

BRIEF SUMMARY OF THE INVENTION

The compounds of this invention are 1-(4-aminophenyl)triazoles optionally substituted on the 3- and 5-positions of the triazole ring and on the amino group on the 4-position of the phenyl ring, having antiinflammatory activity by virtue of their ability to inhibit IL-2 production in T-lymphocytes.

In its broadest generic aspect, the invention comprises 1-(4-aminophenyl)triazoles of Formula I

wherein:

R₁ and R₂, which may be the same or different, are CF₃; halogen; CN; branched or unbranched C₁₋₈ alkyl; branched or unbranched C₁₋₈ alkenyl; C₃₋₈ cycloalkyl optionally substituted with OH, CN or methoxy; C₁₋₈ alkoxy; C₁₋₄ alkyloxyalkyl; C₁₋₈ alkylthio; C₁₋₄ alkylthioalkyl; C₁₋₈ dialkylamino; C₁₋₄ dialkylaminoalkyl; CO₂R₄ where R₄ is C₁₋₄ alkyl or C₁₋₄ alkenyl optionally substituted with carbocyclyl or heterocyclyl; aryl or heterocyclyl connected to the imidazole in any position that makes a stable bond which aryl or heterocyclyl may be optionally substituted with halogen, C₁₋₄ alkyl, C₁₋₄ alkenyl, CN, Me₂N, CO₂Me, OMe, aryl, heterocyclyl or R₄;

L is —NHC(O)—; —NHC(O)O—; —NHC(O)C(O)—; —NHC(S)—; —NH—; —NHC(O)NH—; —NHC(S)NH—; —NHCH—₂; —NHCH(R₅)— where R₅ is H, CN, C₁₋₆ alkyl, C₁₋₆ alkyloxyoalkyl C₁₋₆ alkythioalkyl, C₁₋₆ alkylsulfinylalkyl, C₁₋₆ alkysulfonylalkyl, C₃₋₆ cycloalkyl, heterocyclyl or aryl optionally substituted with a halogen, C₁₋₄ alkyl, CN, Me₂N, CO₂Me or OMe; or L is —NHC(R₅)-lower alkyl;

R₃ is C₁₋₈ alkyl; C₁₋₈ alkyloxy; C₁₋₈ alkylthio; C₁₋₈ alkylamino; C₁₋₄ alkoxyalkyl; C₁₋₄ alkylthioalkyl; C₁₋₄ alkylaminoalkyl, C₁₋₄ dialkylalkylaminoalkyl; carbocyclyl or heterocyclyl, which carbocyclyl or heterocyclyl may optionally be substituted with one or more of the following:

halogen, —CN, —NO₂, —SO₂NH₂ or R₆ (where R₆ is phenyl, heterocyclyl, C₃₋₆-cyucloalkyl, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₁₋₆-alkyloxyalkyl, C₁₋₆-alkylthioalkyl, C₁₋₆-alkylsulfinylalkyl, C₁₋₆-alkylsulfonylalkyl or C₂₋₆-alkynyl) and R₆ may be optionally substituted with halogen, —OH, alkyloxy, —CN, —COO-lower alkyl, —CONH-lower alkyl, —CON (lower alkyl)₂, dialkylamino, phenyl or heterocylcyl; or R₃ is —CO₂R₆; —N(R₆)2; —NH(R₆); —C(O)R₆; —OR₆; S(O)_(n)R₆ where n is 0, 1 or 2; —SO₂NHR₆; or —SO₂N(R₆)₂; or a pharmaceutically acceptable derivative thereof

DETAILED DESCRIPTION OF THE INVENTION

In order that the invention herein described may be more fully understood, the following detailed description is set forth. As used herein, the following abbreviations are used:

DMAP is 4-dimethylamino pyridine;

DMF is dimethylformamide;

DMSO is dimethylsulfoxide;

Et is ethyl;

EtOAc is ethyl acetate;

Me is methyl;

MeOH is methanol;

THF is tetrahydrofuran; and

EDC is 1-(3-dimethylaminopropyl)-3-ethylcarbodimide hydrochloride.

Also, as used herein, each of the following terms, used alone or in conjunction with other terms, are defined as follows (except where noted to the contrary):

The term “alkyl” refers to a saturated aliphatic radical containing from one to ten carbon atoms. “Alkyl” refers to both branched and unbranched alkyl groups. Preferred alkyl groups are straight chain alkyl groups containing from one to eight carbon atoms and branched alkyl groups containing from three to eight carbon atoms. More preferred alkyl groups are straight chain alkyl groups containing from one to six carbon atoms and branched alkyl groups containing from three to six carbon atoms. “Alkyl”, as used herein, includes unsubstituted alkyl radicals, those radicals that are partially or fully halogenated and those radicals substituted with one to four, preferably one or two, substituents selected from amino, cyano, nitro, methoxy, ethoxy and hydroxy. The term “cycloalkyl” refers to the cyclic analog of an alkyl group, as defined above. Preferred cycloalkyl groups are saturated cycloalkyl groups containing from three to eight carbon atoms, and more preferably three to six carbon atoms. “Alkyl” and “cycloalkyl”, as used herein, include unsubstituted alkyl and cycloalkyl radicals, those radicals that are partially or fully halogenated and those radicals substituted with one to four, preferably one or two, substituents selected from halo, amino, cyano, nitro, methoxy, ethoxy and hydroxy. It should be understood that any combination term using an “alk” or “alkyl” prefix refers to analogs according to the above definition of “alkyl”. For example, terms such as “alkoxy” or “alkythio” refer to alkyl groups linked to a second group via an oxygen or sulfur atom.

The terms “alkenyl” and “alkynyl” refer to a mono- or polyunsaturated aliphatic hydrocarbon radical containing from two to twelve carbon atoms, containing at least one double or triple bond, respectively. “Alkenyl” and “alkynyl” refer to both branched and unbranched alkenyl and alkynyl groups. Preferred alkenyl and alkynyl groups are straight chain alkenyl or alkynyl groups containing from two to eight carbon atoms and branched alkenyl or alkynyl groups containing from five to ten carbon atoms. More preferred alkenyl and alkynyl groups are straight chain alkenyl or alkynyl groups containing from two to six carbon atoms and branched alkenyl or alkynyl groups containing from five to eight carbon atoms. “Alkenyl” and “alkynyl”, as used herein, include unsubstituted alkenyl or alkynyl radicals, those radicals that are partially or fully halogenated and those radicals substituted with one to four, preferably one or two, substituents selected from halo, amino, cyano, nitro, methoxy, ethoxy and hydroxy.

The term “aryl” refers to phenyl and naphthyl, phenyl and naphthyl that are partially or fully halogenated and phenyl and naphthyl substituted with halo, alkyl, hydroxy, nitro, —COOH, —CO(lower alkoxy), —CO(lower alkyl), amino, alkylamino, dialkylamino, alkoxy, —NCOH, —NCO(lower alkyl), —NSO₂-Ph(halo)₀₋₃, Ph, —O-Ph; naphthyl, —O-naphthyl, pyrrolyl, pyrrolyl substituted with lower alkyl, pyridyl, pyridinyl, pyrazinyl, pyrimidinyl and pyridazinyl.

The term “halo” refers to a halogen radical selected from fluoro, chloro, bromo or iodo. Preferred halo groups are fluoro, chloro and bromo.

The term “carbocyclyl” refers to a stable 3-8 membered (but preferably 5 or 6 membered) monocyclic or 7-11 membered bicyclic radical which may be either saturated or unsaturated, aromatic or non-aromatic. Preferred carbocycles include, for example, phenyl, naphthyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, indanyl, indenyl, dihydronaphthyl and tetrahydronaphthyl. Most preferred heterocycles of this invention are phenyl, naphthyl, cyclohexyl, tetrahydronaphthyl and indanyl. “Carbocyclyl” refers to unsubstituted carbocyclic radicals, those radicals that are partially or fully halogenated and those radicals substituted with alkyl; hydroxyl; nitro; —COOH; —CO(lower alkoxy); —CO(lower alkyl); amino; alkylamino; dialkylamino; alkoxy; —NCHO; —NCO(lower alkyl); —NSO₂-Ph(halo)₀₋₃, Ph; —O-Ph; naphthyl; —O-naphthyl; pyrrolyl; pyrrolyl substituted with lower alkyl; pyridyl; pyridinyl; pyrazinyl; pyrimidinyl and pyridazinyl.

The term “heterocycle” refers to a stable 5-8 membered (but preferably 5 or 6 membered) monocyclic or 8-11 membered bicyclic heterocycle radical which may be either saturated or unsaturated, aromatic or non-aromatic, and which may be optionally benzo- or pyridofused if monocyclic. Each heterocycle consists of carbon atoms and from 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur. As used herein, “nitrogen” and “sulfur” include any oxidized form of nitrogen and sulfur and the quaternized form of any basic nitrogen. The heterocycle may be attached by any atom of the cycle, which results in the creation of a stable structure. Preferred heterocycles include, for example, benzimidazolyl, furyl, imidazolyl, imidazolinyl, imidazolidinyl, quinolinyl, isoquinolinyl, indolyl, oxazolyl, pyridyl, pyrrolyl, pyrrolinyl, pyrazolyl, pyrazinyl, pyrimidinyl, pyridazinyl, quinoxolyl, piperidinyl, morpholinyl, thiomorpholinyl, furyl, thienyl, triazolyl, thiazolyl, β-carbolinyl, tetrazolyl, thiazolidinyl, benzofuranoyl, thiomorpholinyl sulfone, benzoxazolyl, oxopiperidinyl, oxopyrrolidinyl, oxoazepinyl, azepinyl, isoxazolyl, tetrahydropyranyl, tetrahydrofuranyl, thiadiazoyl, benzodioxolyl, tetrahydrothiophenyl and sulfolanyl. Most preferred heterocycles of this invention include imidazolyl, pyridyl, pyrrolyl, pyrazolyl, piperidinyl, morpholinyl, furyl, thienyl, thiazolyl and the benzo- and pyrido-fused derivatives thereof. “Heterocyclyl” refers to unsubstituted heterocycle radicals, those radicals that are partially or fully halogenated and those radicals substituted with alkyl, hydroxyl, nitro, —COOH, —CO(lower alkoxy), —CO(lower alkyl), amino, alkylamino, dialkylamino, alkoxy, —NCHO, —NCO(lower alkyl), —NSO₂-Ph(halo)₀₋₃, Ph, —O-Ph, naphthyl, —O-naphthyl, pyrrolyl, pyrrolyl substituted with lower alkyl, pyridyl, pyridinyl, pyrazinyl, pyrimidinyl and pyridazinyl.

The term “lower” used in conjunction with other terms (e.g., “alkyl”, “alkoxy” and the like) refers to a radical containing from one to six, preferably from one to five and more preferably, from one to four carbon atoms. For example, a “lower alkyl” group is a branched or unbranched alkyl radical containing from one to six carbon atoms.

The term “patient” refers to a warm-blooded animal, and preferably a human. The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable adjuvant” refers to a non-toxic carrier or adjuvant that may be administered to a patient together with a compound of this invention and which does not destroy the pharmacological activity of that compound.

It should be understood that any compounds of this invention containing one or more asymmetric carbon atoms may occur as racemates and racemic mixtures, single enantiomers, diastereomeric mixtures and individual diastereomers. All such isomeric forms of these compounds are expressly included in the present invention. Each stereogenic center may be in the R or S configuration, or a combination of configurations.

The compounds of this invention are defined to include pharmaceutically acceptable derivatives thereof. A “pharmaceutically acceptable derivative” refers to any pharmaceutically acceptable salt, ester, or salt of an ester of a compound of this invention, or any other compound which, upon administration to a patient, is capable of providing (directly or indirectly) a compound of this invention, a pharmacologically active metabolite or pharmacologically active residue thereof.

Combinations of substituents and variables encompassed by this invention are only those that result in the formation of stable compounds. The term “stable” as used herein, refers to compounds which possess stability sufficient to permit manufacture and administration to a patient by conventional methods known in the art. Typically, such compounds are stable at a temperature of 40° C. or less, in the absence of moisture or other chemically reactive conditions, for at least a week.

The compounds of this invention may be used in the form of salts derived from inorganic or organic acids. Included among such acid salts, for example, are the following: acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, pectinate, persulfate, 3-phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, tosylate and undecanoate.

This invention relates to substituted 1-(4-aminophenyl)triazoles and analogs thereof that inhibit interleukin-2 (IL-2) production. In one embodiment, this invention relates to a novel class of substituted 1-(4-aminophenyl)triazoles and pharmaceutical compositions comprising these compounds. Because of their selective immunomodulating properties, the compounds and pharmaceutical compositions of this invention are particularly well suited for preventing and treating immune disorders, including autoimmune disease, inflammatory disease, organ transplant rejection and other disorders associated with IL-2 mediated immune response.

The substituted 1-(4-aminophenyl)triazoles of this invention are represented by Formula I

wherein:

R₁ and R₂, which may be the same or different, are CF₃; halogen; CN; branched or unbranched C₁₋₈ alkyl; branched or unbranched C₁₋₈ alkenyl; C₃₋₈ cycloalkyl optionallyl substituted with OH, CN or methoxy; C₁₋₈ alkoxy; C₁₋₄ alkyloxyalkyl; C₁₋₈ alkylthio; C₁₋₄ alkylthioalkyl; C₁₋₈ dialkylamino; C₁₋₄ dialkylaminoalkyl; CO₂R₄ where R₄ is C₁₋₄ alkyl or C₁₋₄ alkenyl optionally substituted with carbocyclyl or heterocyclyl; aryl or heterocyclyl connected to the imidazole in any position that makes a stable bond which aryl or heterocyclyl may be optionally substituted with halogen, C₁₋₄ alkyl, C₁₋₄ alkenyl CN, Me₂N, CO₂Me, OMe, aryl, heterocycly or R₄;

L is —NHC(O)—; —NHC(O)O—; —NHC(O)C(O)—; —NHC(S)—; —NH—; —NHC(O)NH—; —NHC(S)NH—; —NHCH—₂; —NHCH(R₅)— where R₅ is H, CN, C₁₋₆ alkyl, C₁₋₆ alkyloxyoalkyl C₁₋₆ alkythioalkyl, C₁₋₆ alkylsulfinylalkyl, C₁₋₆ alkysulfonylalkyl , C₃₋₆ cycloalkyl, heterocyclyl or aryl optionally substituted with a halogen, C₁₋₄ alkyl, CN, Me₂N, CO₂Me or OMe; or L is —NHC(R₅)-lower alkyl;

R₃ is C₁₋₈ alkyl; C₁₋₈ alkyloxy; C₁₋₈ alkylthio; C₁₋₈ alkylamino; C₁₋₄alkoxyalkl; C₁₋₄ alkythialkl; C₁₋₄ alkylamioalkyl; C₁₋₄ dialkylalkylaminoalkyl; carbocyclyl or heterocyclyl, which carbocyclyl and heterocyclyl may optionally be substituted with one or more of the following: halogen, —CN, —NO₂, —SO₂NH₂ or R₆ (where R₆ is phenyl, heterocyclyl, C₃₋₆ cycloalkyl, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₁₋₆ alkyloxyalkyl, C₁₋₆ alkylthioalkyl, C₁₋₆ alkylsulfinylalkyl, C₁₋₆ alkylsulfonylalkyl or C₂₋₆ alkynyl) and R₆ may be optionally substituted with halogen, —OH, alkyloxy, —CN, —COO-lower alkyl, —CONH-lower alkyl, —CON (lower alkyl)₂, dialkylamino, phenyl or heterocylcyl; or R₃ is —CO₂R₆; —N(R₆)2; —NH(R₆); —C(O)R₆; —OR₆; S(O)_(n)R₆where n is 0, 1 or 2; —SN₂NHR₆; or —SO₂N(R₆)₂; or a pharmaceutically acceptable derivative thereof

Preferably, the novel substituted 1-(4-aminophenyl)triazoles of Formula I are those wherein:

R₁ is straight-chained, branched or cyclo-C₃₋₈ alkyl, alkenyl, or alkynyl; C₁₋₃ alkyloxyalkyl, C₁₋₅alkyloxy, C₁₋₃alkylthioalkyl, C₁₋₅ alkylthio, CF₃; heterocyclyl or aryl optionally substituted with halogen, C₁₋₄ alkyl, CN, alkoxy or Me₂N;

R₂ is halogen, Me, Et, CF₃, CN, cyclopropyl, vinyl, SMe, OMe, heterocyclyl or aryl optionally substituted with halogen, C₁₋₄ alkyl, CN, alkoxy or Me₂N;

L is —NHC(O)—, —NH—, —NHC(O)NH, or —NHCH(R₅)—, where R₅ is H, C₁₋₄ alkyl, or CN and

R₃ is C₁₋₆ alkyl; C₁₋₄ alkyloxyalkyl; C₁₋₄ alkylthioalkyl; cyclohexyl; cyclopentyl; indanyl; indolyl; phenyl; thienyl; naphthyl; isoxazolyl; or pyridyl any of which may be optionally substituted with one or more halogen, —CN, —NO₂, SO₂NH₂, or R₆ (where R₆ is C₁₋₆ alkyl, C₂₋₆ alkenyl, C₁₋₆ alkyloxyalkyl, C₁₋₆ alkylthioalkyl, or C₂₋₆ alkynyl) and R₆ may be optionally substituted with OH, CN, —COO-lower alkyl, —CONH-lower alkyl, —CON(lower alkyl)₂, dialkylamino, or heterocycyl; CO₂R₆; —N(R₆)₂, —NH(R₆); —C(O)R₆; —OR₆, S(O)_(n)R₆ where n 0, 1 or 2; —SO₂NHR₆; or —SO₂N(R₆)₂.

More preferred are novel substituted 1-(4-aminophenyl)triazoles of Formula I wherein:

R₁ is Et, i-Pr, n-Pr, t-Bu, cyclopentyl, CF₃, —OEt, MeOCH₂—, 2- or 3-tetrahydrofuranyl, 2-, 3-, or 4-pyridyl, 2-furanyl, or 2-thiazolyl;

R₂ is CN, CF₃, Cl, Me, Et, SMe, cyclopropyl, vinyl, or 2-furanyl;

L is —NHC(O)—, —NH— or —NHCH₂—; and

R₃ is a phenyl ring which is optionally substituted with one to three groups selected from C₁₋₃alkyl, chloro, fluoro, CF₃, OC₁₋₄alkyl, OC₃₋₅alkenyl, CO₂C₁₋₂alkyl, SMe, CN, NO₂, NMe₂ and O(CH₂)_(p)R₇, where p is 3 or 4 and R₇ is CN, CO₂Me, 2-(1,3-dioxolanyl), OH, or OC₆H₅; 1 or 2-indanyl, 2-tetrahydropyranyl, or a heterocycle selected from the group consisting of 2-thienyl, 3-furanyl, 3- or 4-pyridyl, 4-isoxazolyl, 1-isoquinolinyl, 2-indolyl, 2-benzothienyl and 4-pyrazolyl, any of which may be optionally substituted with one to three groups selected from Cl, Br, Me, CN, CF₃, OCF₃, NO₂, or O(CH₂)_(p)R₇, where p is 3 or 4 and R₁₃ is CN, CO₂Me, 2-(1,3-dioxolanyl), OH, or OC₆H₅; C₅₋₆ alkyl; C₅₋₆cycloalkyl; or cyclohexenyl.

Especially preferred are novel substituted 1-(4-aminophenyl)triazoles of Formula I wherein:

R₁ is i-Pr, CF₃, 3-pyridyl or 4-pyridyl;

R₂ is CN, CF₃, Cl, Me, SMe or Et;

L is —NHC(O)—, —NH— or —NHCH₂—; and

R₃ is a phenyl ring which is optionally substituted with O(CH₂)₃R₈, where R₈ is CN, OH or 2-(1,3-dioxolanyl); OC₃₋₄alkyl; O(CH₂)₄OH; 1-pentenyl substituted with one to three groups selected from Me, Cl, F and CN; 3-pyridyl optionally substituted in the 6-position with O(CH₂)₂OEt or O(CH₂)₃R₈, where R₈ is CN, OH or 2-(1,3-dioxolanyl); 4-pyridinyl optionally substituted with a chlorine; 2-thienyl optionally substituted with Me or Br; 3,5-dimethyl-4-isoxazolyl; 1-methyl-2-indolyl; cyclopentyl; cyclohexyl; 1-indanyl; or n-pent-3-yl.

Compounds of Formula I in which L is —NHC(O)— may be prepared by one of the methods outlined below. For example, a (4-aminophenyl)-3,5-disubstituted triazole 1 may be reacted with a carboxylic acid 2 under suitable coupling conditions known to one skilled in the art, for example in the presence of EDC and a base catalyst such as N,N-dimethylaminopyridine in a suitable solvent such as methylene chloride, acetonitrile or DMF (Method A). Alternatively, 1 could be coupled with an acid halide 3 in the presence of a suitable base such as triethylamine in a suitable solvent such as methylene chloride (Method B).

Compounds of formula I in which L is —NH— and R₃ is a heteroaryl ring may be prepared, as illustrated below, by reaction of a (4-aminophenyl)-3,5-disubstituted triazole 1 with a heterocycle 4 containing a labile substituent such as a halogen, which may be displaced by nucleophilic substitution (Method C). The reaction may be carried out in a sealed tube or an open vessel, at ambient temperature or heated to 150° C. in a suitable solvent such as dioxane or THF. A base such as sodium bis-trimethylsilyl amide may be added to the reaction.

Compounds in which L is —NHC(O)NH— may be prepared by reaction of isocyanate 5 with an amine 6 in a suitable solvent such as methylene chloride or toluene (Method D). An amine such as triethylamine may be added. Alternatively, 1 could be reacted with an amine carbonyl chloride such as N-morpholine carbonyl chloride 7 in a suitable solvent such as methylene chloride (Method E). Intermediates 5 may be prepared from the corresponding 1 by methods known to those skilled in the art, for example by reaction of 1 with phosgene or a phosgene equivalent in the presence of a suitable base such as potassium carbonate, in a suitable solvent, such as methylene chloride.

Methods by which compounds in which L is —NHCH(R,)— or —NHCH₂ may be prepared are illustrated below. For example, these compounds may be prepared by reduction of the corresponding amide (L is —NHC(O)—) with a suitable reducing agent such as lithium aluminum hydride, in a suitable solvent such as THF or diethyl ether (Method F). Alternatively, amine 1 could react with an alkylating agent 8 (Method G) where X is a suitable leaving group such as a halogen. In another alternate procedure, amine 1 could react with an aldehyde 9, and the intermediate imine 10 reacted with a reducing agent such as sodium cyanoborohydride or sodium triacetoxyborohydride (Method H). Alternatively, 10 could be reacted with a nucleophile such as an alkyl or aryl lithium reagent (Method I).

Preparation of intermediates used in the above procedures may be done by methods known to those skilled in the art and described in the chemical literature. For example, a 3,5-disubstituted triazole may be reacted with nitrobenzene substituted in the 4-position with a leaving group such as a halogen in the presence of a base (Method J). The nitrophenyltriazoles produced could then be reduced to aminophenyl triazoles by using a reducing agent such as SnCl₂ or hydrogen or a hydrogen source such as ammonium formate in the presence of a catalyst such as palladium.

Procedures described by M. A. Perez et al. (Synthesis, 1983, 483) may also be used to prepare desired intermediates 1 as illustrated in Methods K and L. An alkyl imidate bearing the desired R. (Method K, 12, R=alkyl) may be reacted with an acyl halide bearing the desired R₂ in a suitable solvent, preferably toluene, in the presence of a suitable base, such as triethyl amine, to provide an alkyl N-acylimidate 13. Reaction of 13 with 4-nitrophenylhydrazine in a suitable solvent, such as carbontetrachloride results in cyclization to 11. This may be reduced to intermediate 1 as described in Method J.

By using methyl chloroformate in place of an acyl chloride, and a suitable base, such as 2,4,6-trimethylpyridine, one may obtain an N-methoxycarbonylimidate 14 (Method L). Reaction of this with 4-nitrophenylhydrazine provides triazol-3-one 15. This is a useful intermediate in preparing additional intermediates with desired R₂. For example, reaction of 15 with a chlorinating agent, such as POCl₃ provides 11 (R₂=Cl). Analogously 11 (R₂=Br) may be prepared using for example POBr₃. Reaction of 11 (R₂=Cl) with sodium thiomethoxide provides 11 (R₂=SMe).

The synthesis of hydroxymethyl intermediate 11 (R₂=CH₂OH) has been reported by E. J. Browne et al. (J. Chem. Soc. C., 1970, 1515), and is illustrated in Method M. Reaction of an acyl isocyanate bearing R₁ (16) with diazomethane provides oxazolinone 17. Reaction of 17 with 4-nitrophenylhydrazine provides 11 (R₂=CH₂OH). This intermediate may be used to prepare additional intermediates 11 with other desired R₂ by standard functional group transformations known to those skilled in the art. For example, oxidation of 11 (R₂=CH₂OH) to the corresponding carboxylic acid (R₂=CO₂H), followed by amide formation (R₂=C(O)NH₂), and dehydration provides 11 (R₂=CN).

A procedure useful in preparing certain pyrazoles with R₁=CF₃ which may be adapted to prepare desired intermediates 11 has been reported by K. H. Pilgram and R. D. Skiles (J. Het. Chem., 1983, 20, 1533). As illustrated in Method N, reaction of phenylhydrazine with cyanogen bromide provides 18. Reaction with H₂S, followed by alkylation with iodomethane provides 19. Reaction of 19 with trichloromethyl trifluoromethyl ketone provides 20. This may be nitrated to give 11 (R₁=CF₃, R₂=SMe). One may prepare additional 11 by hydrolysis to 21 followed by chlorination or bromination as described for 15 in Method L.

Several additional intermediates could be obtained from the 5-bromotriazole 11 (R₂=Br) (prepared as described in Method L or N) as illustrated below in M. For example, as illustrated in Method O, 11 (R₂=Br) may be cross coupled with a terminal acetylene 22, where Z may be, for example, hydrogen or an alkyl group or any other group not adversely affecting the reaction, using conditions described by T. Sakamoto et al., (Synthesis, 1983, 312) to provide 11 with an alkyne at R₂. Alternatively, reaction with vinylstannanes 23, Z defined as above, under conditions described by J. W. Stille (Angew. Chem. Int. Ed. Engl., 1986, 25, 508), provides 11 with an alkene at R₂ ( Method P). Reaction with substituted or unsubstituted aryl- or heteroarylboronic acids (24) under conditions described by N. Miyaura et al. (Chem. Rev. 1995, 95, 2457) provides 11 with aryl or heteroaryl groups at R₂ (Method Q). Alkynes and alkenes may be converted to the corresponding alkyl groups by reduction with a suitable reducing agent such as hydrogen in the presence of a suitable catalyst such as platinum or palladium (see Method J) to provide desired 1, with an alkyl group at R₂.

Alternatively, reaction with a reducing agent that leaves alkenes and alkynes intact, such as SnCl₂ provides 1 with alkenes or alkynes at R₂.

a. Pd(PPh₃)₄, CuBrSMe₂, Et₃N b. Pd(PPh₃)₄, THF c. Pd(PPh₃)₄, 2M Na₂CO₃, THF

Method R describes an alternate procedure for preparing compounds of Formula I where L is —NH—. Intermediate 1 may be heated at about 70° C. with an aryl bromide in the presence of a palladium catalyst, preferably Pd₂(dba)₃, 2,2′-bis(diphenylphosphino)-1,1′-binapthyl (BINAP), and a base, preferably NaOt-Bu, in a solvent such as toluene, as described by S. Buchwald et al.(J. Amer. Chem. Soc., 1993, 119, 8451). Alternately, one could employ the same conditions with the bromophenyltriazole 25 and an amine, R₃NH₂.

As can be appreciated by chemists possessing ordinary skill in the art, the synthetic schemes described above are for illustrative purposes only and may be modified using conventional synthetic methodology to produce any of the analogs of Formula I. Depending on precisely how the synthetic schemes are modified, the specific reaction conditions might also require modification. Such modifications may involve the use of higher or lower temperature or pressure, conditions other than those reported herein, or the addition of further synthetic steps such as functional group transformations. However, since progress of the reactions is easily monitored by techniques such as high performance liquid chromatography, gas chromatography, mass spectroscopy, thin layer chromatography, nuclear magnetic resonance spectroscopy and the like, such modifications are well within the skill of the art. Likewise, it should be appreciated that initial products from these Methods could be further modified to make additional compounds of this invention. Intermediates used in the Methods described above may be commercially available or could be prepared from commercially available sources by methods described in the chemical literature and known to people skilled in the art.

The 1-phenyltriazole analogs of Formula I inhibit production of IL-2. Without wishing to be bound by theory, the compounds of this invention inhibit IL-2 production by T cells. This inhibition of IL-2 production is therapeutically useful for selectively suppressing immune function. The result of such selectively suppressed immunity includes reduced cell proliferation of peripheral blood lymphocytes and cellular immune response. Thus, the inhibition of IL-2 production is an attractive means for preventing and treating a variety of immune disorders, including inflammatory diseases, autoimmune diseases, organ and bone marrow transplant rejection and other disorders associated with IL-2 mediated immune response. In particular, the compounds of Formula I may be used to prevent or treat acute or chronic inflammation, allergies, contact dermatitis, psoriasis, rheumatoid arthritis, multiple sclerosis, type 1 diabetes, inflammatory bowel disease, Guillain-Barre syndrome, Crohn's disease, ulcerative colitis, graft versus host disease (and other forms of organ or bone marrow transplant rejection) and lupus erythematosus. Other disorders associated with IL-2 mediated immune response will be evident to those of ordinary skill in the art and can also be treated with the compounds and compositions of this invention.

The compounds of this invention may be administered in any conventional dosage form in any conventional manner. Such methods of treatment, including their dosage levels and other requirements, may be selected by those of ordinary skill in the art from available methods and techniques. For example, a compound of this invention may be combined with a pharmaceutically acceptable carrier or adjuvant for administration to a patient in need of such treatment in a pharmaceutically acceptable manner and in an amount effective to treat (including lessening the severity of symptoms) the immune disorder.

The compounds of this invention may be administered alone or in combination with conventional therapeutics, such as conventional immunosuppressants. Advantageously, such combination therapies utilize lower dosages of the conventional therapeutics, thus avoiding possible toxicity and adverse side effects incurred when those agents are used as monotherapies. The compounds of this invention may be physically combined with the conventional therapeutics into a single pharmaceutical composition. Advantageously, the compounds may then be administered together in a single dosage form. Alternatively, the compounds may be administered separately (either serially or in parallel). Separate dosing allows for greater flexibility in the dosing regime.

According to this invention, the compounds of Formula I and the pharmaceutical compositions containing those compounds may be administered to a patient in any conventional manner and in any pharmaceutically acceptable dosage from, including, but not limited to, intravenously, intramuscularly, subcutaneously, intrasynovially, by infusion, sublingually, transdermally, orally, topically or by inhalation. The preferred modes of administration are oral and intravenous.

Dosage forms of the compounds of this invention include pharmaceutically acceptable carriers and adjuvants known to those of ordinary skill in the art. These carriers and adjuvants include, for example, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, buffer substances, water, salts or electrolytes and cellulose-based substances. Preferred dosage forms include, tablet, capsule, caplet, liquid, solution, suspension, emulsion, lozenges, syrup, reconstitutable powder, granule, suppository and transdermal patch. Methods for preparing such dosage forms are known (see, for example, H. C. Ansel and N. G. Popovish, Pharmaceutical Dosage Forms and Drug Delivery Systems, 5th ed., Lea and Febiger (1990)). Dosage levels and requirements are well-recognized in the art and may be selected by those of ordinary skill in the art from available methods and techniques suitable for a particular patient. Typically, dosage levels range from about 10-1000 mg/dose for a 70 kg patient. Although one dose per day may be sufficient, up to 5 doses per day may be given. For oral doses, up to 5000 mg/day may be required. As the skilled artisan will appreciate, lower or higher doses may be required depending on particular factors. For instance, specific dosage and treatment regimens will depend on factors such as the patient's general health profile, the severity and course of the patient's disorder or disposition thereto and the judgment of the treating physician.

SYNTHETIC EXAMPLES

In order that this invention be more fully understood, the following examples are set forth. These examples are for the purpose of illustrating preferred embodiments of this invention, and are not to be construed as limiting the scope of the invention in any way.

Example 1 Synthesis of N-[4-(5-Methylthio-3-pyridin-4-yl)-1H-1,2,4-triazol-1-yl)phenyl]pyridine-3-carboxamide

A suspension of 5-(4-pyridyl)-1H-1,2,4-triazole-3-thiol (Aldrich) (4 g, 22.4 mmol) and .potassium t-butoxide (2.89 g, 25.8 mmol) in DMF (30 mL) was stirred at room temperature under argon until a homogeneous solution resulted. Methyl iodide (1.48 mL 23.8 mmol) was added and the reaction mixture was heated to 50° C. in an oil bath for 16 h. The reaction mixture was diluted with water, extracted with EtOAc, the organic extract was washed with water and dried (MgSO₄). The solid obtained on concentration was filtered from hot ethyl acetate to obtain 3-methylthio-5-(4-pyridyl)-1H-1,2,4-triazole (1.97 g).

A solution of the methylthiotriazole from above (1 .91g, 9.9 mmol) and potassium t-butoxide (1.16 g, 10.4 mmol) in anhydrous DMSO (15 mL) was stirred at room temperature for 5 min and then 4-flouronitrobenzene (1.04 mL, 9.9 mmol) was added. The reaction mixture was heated to 100° C. in an oil bath for 5 h under argon. The reaction mixture was cooled, diluted with water, the solid obtained was filtered, washed with water and dried. The residue obtained was filtered from hot MeOH to give 5-methylthio-1-(4-nitrophenyl)-3-(4-pyridyl)-1H-1,2,4-triazole (2.75 g).

To a stirred suspension of the nitrophenyltriazole from above (1 g, 3.1 mmol) in glacial acetic acid (20 mL) was added a solution of SnCl₂.2H₂O (5.04 g, 22.3 mmol) in concentrated HCl (8 mL) and the reaction was stirred for 36 h at room temperature. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water (4×), dried (MgSO₄) and concentrated to give 1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazole (0.87 g).

A mixture of the amine from above (0.45 g, 1.58 mmol), nicotinic acid (0.293 mg, 2.38 mmol) and EDC (0.502 g, 2.62mmol) was dissolved in 10 mL of acetonitrile. DMAP (10 mg) was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted with water, the solid obtained was filtered, washed with water and dried. The residue obtained was filtered from hot MeOH to give the title compound (0.6 g), mp. 226-8° C.

Example 2 Synthesis of (3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amine

A stirred solution of 1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazole (Example 1) (100 mg, 0.35 mmol) and 3-methylthiophene-2-carboxaldehyde (44 mg, 0.35 mmol) in 5% acetic acid in MeOH (4 mL) at room temperature was treated with sodium cyanoborohydride (55 mg, 0.88 mmol) and the reaction mixture was further stirred at room temperature for 48 h. The reaction mixture was concentrated, diluted with EtOAc, washed with NaHCO₃ solution, brine and dried (MgSO₄). The residue obtained on concentration was flash chromatographed on silica gel and eluted with a gradient of dichloromethane/acetone (9/1 to 3/1). The title compound was obtained as a white solid (85 mg).

Assessment of Biological Properties IL-2 Promoter Assay

The IL-2 promoter assay measures transcriptional activation of a luciferase reporter gene which has been placed under control of the IL-2 promoter/enhancer. All the known regulatory features of the IL-2 gene are contained within a ˜300 bp sequence immediately upstream of the open reading frame. The region −328 to +35 relative to the transcription start site of the IL-2 gene is obtained by RT-PCR of human genomic DNA and is subcloned into the promoterless luciferase reporter vector pGL2-Basic (Promega). The resulting construct, pIL2P-luc, and a vector containing a neomycin resistance gene, pcDNA/Neo (Invitrogen), are linearized and stably transfected into Jurkat cells (a human T cell line) by electroporation. Following G-418 selection and dilution cloning, a cell line was established, J.1F/C6. , which exhibited a strong induction of luciferase activity upon treatment with ionomycin and PMA (up to 100-fold), and potent inhibition by FK506 (IC₅₀=0.3 nM).

For screening compounds, the cells are pelleted by centrifugation, washed once with PBS, resuspended in RPMI (phenol red-free) containing 5% FBS, and dispensed into 96-well, white microtiter plates (Packard) at 50,000 cells/well. The cells are pre-incubated with compounds (1 μg/ml) for 15 min prior to addition of ionomycin (1 μg/ml) and PMA (10 ng/ml) in a final volume of 100 μl. Following a 5 hr incubation at 37° C. in a humidified incubator, 100 μl of Luc-Lite lysis buffer/luciferase assay buffer (Promega) is added and luminescence measured using a Packard TopCount scintillation counter/luminometer.

The compounds described in Synthetic Examples 1 and 2 were screened in this assay and had IC₅₀ values below 10 microM

While we have described a number of embodiments of this invention, it is apparent that our basic constructions may be altered to provide other embodiments which utilize the products and methods of this invention. Therefore, it will be appreciated that the scope of this invention is to be defined by the appended claims, rather than by the specific embodiments that have been presented herein by way of example. 

What is claimed is:
 1. A compound of formula (I)

wherein: R₁ is pyridyl optionally substituted with halogen, C₁₋₄ alkyl, C₂₋₄ alkenyl, CN, Me₂N, CO₂Me, OMe, aryl, or R₄; R₂ is halogen, Me, Et, CF₃, CN, cyclopropyl, vinyl, SMe, OMe, or aryl optionally substituted with halogen, C₁₋₄ alkyl, CN, alkoxy, or Me₂N, L is —NHC(O)—, —NH—, —NHC(O)NH, or —NHCH(R₅)—, wherein R₅ is H, C₁₋₄ alkyl, or CN; and R₃ is C₁₋₄ alkyl; C₁₋₄ alkyloxyalkyl; C₁₋₄ alkylthioalkyl; cyclohexyl, cyclopentyl, indanyl, indolyl, phenyl, thienyl, naphthyl, isoxazolyl, or pyridyl optionally substituted with one or more halogen, —CN, —NO₂, SO₂NH₂, or R₆, wherein R₆ is C₁₋₄ alkyl, C₂₋₄ alkenyl, C₁₋₆ alkyloxyalkyl, C₁₋₆ alkylthioalkyl, or C₂₋₆ alkynyl, and R₆ is optionally substituted with OH, CN, —COO-lower alkyl, —CONH-lower alkyl, —CON(lower alkyl)₂, dialkylamio, or CO₂R₆; —N(R₆)₂; —NH(R₆); —C(O)R₆; —OR₆; S(O)_(n)R₆, wherein n is 0, 1, or 2; —SO₂NHR₆; or —SO₂N(R₆)₂; and R₄ is C₁₋₄ alkyl or C₂₋₄ alkenyl optionally substituted with carbocyclyl, or a pharnaceutically acceptable derivative thereof.
 2. A compound of formula (I)

wherein: R₁ is 2-, 3-, or 4-pyridyl; R₂ is CN, CF₃, Cl, Me, Et, SMe, cyclopropyl, or vinyl; L is —NHC(O)—, —NH—, or —NHCH₂—; and R₃ is a phenyl ring which is optionally substituted with one to three groups selected form C₁₋₃alkyl, chloro, fluoro, CF₃, OC₁₋₄alkyl, OC₃₋₅alkenyl, CO₂C₁₋₂alkyl, SMe, CN, NO₂, NMe₂ and O(CH₂)_(p)R₇, where p is 3 or 4 and R₇ is CN, CO₂Me, 2-(1,3-dioxolanyl), OH, or OC₆H₅; 1- or 2-indanyl, 2-tetrahydropyranyl, or a heterocycle selected from the group consisting of 2-thienyl, 3-furanyl, 3- or 4-pyridyl, 4-isoxazolyl, 1-isoquinolinyl, 2-indolyl, 2-benzothienyl and 4-pyrazolyl, which may be optionally substituted with one to three groups selected from Cl, Br, Me, CN, CF₃, OCF₃, NO₂, or O(CH₂)_(p)R₇, where p is 3 or 4 and R₇ is CN, CO₂Me, 2-(1,3-dioxolanyl), OH, or OC₆H₅, or R₃ is C₅₋₆ alkyl, C₅₋₆cycloalkyl or cyclohexenyl; and R₄ is C₁₋₄ alkyl or C₂₋₄ alkenyl optionally substituted with carbocyclyl, or a pharmaceutically acceptable derivative thereof.
 3. A compound of formula (I)

wherein: R₁ is 3-pyridyl or 4-pyridyl; R₂ is CN, CF₃, Cl, Me, SMe, or Et; L is —NHC(O)—, —NH—, or —NHCH₂—; and R₃ is a phenyl ring optionally substituted with O(CH₂)₃R₈, where R₈ is CN, OH, or 2-(1,3-dioxolanyl); OC₃₋₄alkyl, O(CH₂)₄OH, 1-pentenyl, one to three groups selected from Me, Cl, F, and CN; 3-pyridyl optionally substituted in the 6-position with O(CH₂)₂OEt or O(CH₂)₃R₈, wherein R₈ is CN, OH, or 2-(1,3-dioxolanyl); 4-pyridinyl optionally substituted with a chlorine, 2-thienyl optionally substituted with Me or Br, 3,5-dimethyl-4-isoxazolyl, 1-methyl-2-indolyl, cyclopentyl, cyclohexyl, 1-indanyl, or n-pent-3-yl; and R₄ is C₁₋₄ alkyl or C₂₋₄ alkenyl optionally substituted with carbocyclyl, or a pharmaceutically acceptable derivative thereof.
 4. A compound selected from the group consisting of: (a) N-[4-(5-Methylthio-3-pyridin-4-yl)-1H-1,2,4-triazol-1-yl)phenyl]pyridine-3-carboxamide; (b) (3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (c) N-[4-(5-Ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]pyridine-3-carboxamide; (d) (2-Chloro-6-fluorobenzyl)-[4-(5-ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (e) (2-Methylbenzyl)-[4-(5-ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (f) [6-(3-Cyanopropoxy)pyridin-3-ylmethyl]-[4-(5-cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (g) [6-(3-[1,3]Dioxolan-2-ylpropoxy)pyridin-3-ylmethyl]-[4-(5-cyano-3-pyridin-1H-1,2,4-triazol-1-yl)phenyl]amine; (h) N-[4-(5-Ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-1-methylindole-2-carboxamide; (i) (2-Chloro-6-fluorobenzyl)-[4-(5-cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (j) [4-(5-Cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-(2,6-dimethylbenzyl)amine; (k) (2-Chloro-6-methylbenzyl)-[4-(5-cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine; (l) [4-(5-Cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-(2-indanylmethyl)amine; (m) [4-(5-Ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-(2-indanylmethyl)amine; (n) [4-(5-Ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-(2-fluoro-6-methylbenzyl)amine; (o) 4-(3-Cyanopropoxy)-N-[4-(5-cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]benzamide; (p) N-[4-(5-Cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]-4-(3-[1,3]dioxolan-2-propoxy)benzamide; (q) [4-(3-Cyanopropoxy)benzyl]-[4-(5-ethyl-3-pyridin-3-yl-1H-1,2,4-triazol-yl)phenyl]amine; and (r) [4-(3-Cyanopropoxy)benzyl]-[4-(5-cyano-3-pyridin-3-yl-1H-1,2,4-triazol-1-yl)phenyl]amine.
 5. A pharmaceutical composition comprising an effective amount of the compound according to claim 1 and a pharmaceutically acceptable carrier or adjuvant.
 6. A method of treating an inflammatory disease which comprises administering to a patient in need of such treatment a therapeutically effective amount of a compound according to claim
 1. 7. A pharmaceutical composition comprising an effective amount of the compound according to claim 2 and a pharmaceutically acceptable carrier or adjuvant.
 8. A pharmaceutical composition comprising an effective amount of the compound according to claim 3 and a pharmaceutically acceptable carrier or adjuvant.
 9. A pharmaceutical composition comprising an effective amount of the compound according to claim 4 and a pharmaceutically acceptable carrier or adjuvant.
 10. A method of treating an inflammatory disease which comprises administering to a patient in need of such treatment a therapeutically effective amount of a compound according to claim
 2. 11. A method of treating an inflammatory disease which comprises administering to a patient in need of such treatment a therapeutically effective amount of a compound according to claim
 3. 12. A method of treating an inflammatory disease which comprises administering to a patient in need of such treatment a therapeutically effective amount of a compound according to claim
 4. 